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Effect of Antihypertensive Drug Therapy on the Blood

Pressure Control among Hypertensive Patients Attending

Campus’ Teaching Hospital of Lome, Togo, West Africa

Yao Potchoo1, Edem Goe-Akue1, Findibe Damorou1, Barima Massoka2, Datouda Redah1, Innocent P. Guissou3

1

University of Lome, Mixed Faculty of Medicine and Pharmacy, Lome, Togo; 2University of Lome, School of Medical Assistants, Lome, Togo; 3University of Ouagadougou, UFR/SOH, Laboratory of Pharmacology/Toxicology, Ouagadougou, Burkina Faso. Email: ypotchoo@hotmail.com

Received January 17th, 2012; revised February 24th, 2012; accepted March 6th, 2012

ABSTRACT

High blood pressure (HBP) is a health problem world-wide. In Togo, that affection constitutes a more and more pre- occupying cause of morbidity and mortality. This study is a prospective one which intended to identify the antihyper- tensive regimens prescribed and evaluate their effect on patients’ blood pressure (BP) control. Out of the 204 patients enrolled (mean: 55.01  12.55 years; sex ratio: 1.3), 112/176 placed on antihypertensive therapy have controlled their BP (38.39% outpatients vs 61.61% inpatients). Related to the sex factor, we didn’t observe any significant difference in the BP control. Whereas, the mean median value of BP reduction of outpatients (30.00/15.00 mmHg) (p = 0.001) was half lower than that of inpatients (60.00/30.00 mmHg (p = 0.004)). Thirty five outpatients (81.40%) vs 64 inpatients (92.75%) were placed on combination therapy. The bitherapy was prescribed to 23 outpatients (53.49%) against 27 in-patients (39.13%) while the quadritherapy and more than 4 drugs combination were prescribed exclusively to inin-patients (20.29%, n = 14). That quadritherapy induced a significant mean reduction of inpatients’ SBP compared to monothe- rapy (p = 0.043) and to bitherapy (p = 0.004). The favorite combinations were D + CCA, D + ACEI, D + CCA + ACEI and D + CCA + ACEI + CAAD of which the quadruple therapy showed a significant inpatients’ DBP control (p = 0.015) compared to D + CCA combination. The combinations including at least one diuretic induced a significant difference between outpatients (median value: 30.000/10.000 mmHg) (p  0.001) and inpatients (median value: 60.000 mmHg/30 mmHg) (p  0.001). The first-line molecules and fixe combinations prescribed in decreasing frequency were among others: hydrochlorothiazide + captopril, nicardipine,  methyldopa for outpatients; furosemide, nicardipine, captopril,  methyldopa, hydrochlorothiazide + captopril for inpatients. Diuretics, CCAs and ACEIs were the 3 favorite pharma-cological groups for essential hypertension management in our African resource limited context. Combined to CAAD, they represented the best quadruple combination among inpatients having showed a significant difference in DBP con-trol compared to D + CCA combination.

Keywords: Antihypertensive Drugs; Ambulatory Patients; Hospitalized Patients; Blood Pressure Control; Prescription; Monotherapy; Bitherapy; Tritherapy; Quadritherapy; CHU-Campus; Togo; West Africa

1. Introduction

Essential high blood pressure (HBP) is a public health problem world-wide due to its prevalence, its asympto- matic character (at the initial stage of the disease), its chronicity, its cerebro vascular and cardio-vascular [1,2], renal complications and its weight in the expenses of health. Many factors among which the low level of adhe- rence for therapeutic schedules, ignorance, poverty [3-5], the role of health staff [6,7] and the complexity of anti hypertensive therapy [8] explain the high rate of the re- sistance to the treatment.

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[12], occupies the best place. However, there are various pharmacological groups with different target, essentially central nervous system, cardiovascular and renal system. Those drugs are used either in monotherapy or most often in combination of 2, 3, 4 drugs belonging to different pharmacological groups hence the difficulty of the choice for a better synergy and a lesser risks. The data of the li- terature estimate that the blood pressure (BP) of 1/3 of patients is controlled by monotherapy, 1/3 by bitherapy and the remaining 1/3 by an antihypertensive drugs num- ber superior or equal to 3 [8]. The HBP pharmacotherapy associated or not with hygieno-dietetic measures, aims at the reduction of BP, cardiovascular risks (myocardial infarction, cerebro-vascular accident and stroke) [13-15] without adversely affecting patients’ quality of life. It re- quires a high level of adherence.

That prospective study, the first of its type in Togo and which has very few data in sub-Saharan Africa, intends to identify the antihypertensive drugs as well as the com- binations of interest which induced the BP control among patients admitted in CHU-Campus Teaching Hospital of Lomé; to evaluate the role of sex factor and the patients’ ambulatory or hospitalized status, to compare the effect of the combinations of different pharmacological groups of antihypertensive drugs on patients’ BP control. The study findings would allow to have some pre-requisites for the elaboration of interventions for antihypertensive drugs use and the improvement of essential HBP mana- gement.

2. Method

2.1. Eligible Patients

The criteria of enrolment were all patient having con- sulted or having been referred or hospitalized at the service of cardiology of Campus’ Teaching hospital and among whose the diagnosis of HBP has been made (BP higher than the limits defined by the Wold Health Orga- nization (WHO)): 140 mmHg for the systolic blood pre- ssure (SBP) and 90 mmHg for the diastolic blood pre- ssure (DBP); patients were submitted to a check-up and then placed on an antihypertensive drug therapy.

Patients with irregular follow up visits, those whose data collected was incomplete or whose adherence was poor and those that claimed to take in addition to the me- dicinal treatment a traditional remedy were excluded from the study.

2.2. Material

To measure the parameters of interest (blood pressure, weight, size) we used:

-Spengler mercury Sphygmomanometer provided with an armband for adult of 12 cm large,

-Spengler Stethoscope, -Height,

-SECA Scales with maximum load of 150 kg.

2.3. Data Collection Method and Variable of Interest

The present survey was prospective covering a period of one year from February 2001 to January 2002. It was conducted among the outpatients and inpatients attending the service of cardiology of Campus’ Teaching Hospital for hypertension conditions. A card of questionnaire allowed us to collect the information concerning the age, the sex, the hospitalized or ambulatory status, the level of the blood pressure before placing them on antihyper- tensive therapy, the antihypertensive therapy regimens applied to patients and then the level of the blood pre- ssure after placing the patients on single drug therapy or combination therapy.

The blood pressure was measured using the ausculta- tory method. The conditions of measurement were the rest condition, the quietness and without emotion.

The status of hypertension control was classified as controlled and uncontrolled hypertension using the limits defined previously. The mean difference between base- line SBP/DBP and that obtained after placing patients on antihypertensive therapy was calculated. These mean dif- ferences were used to compare treated groups.

2.4. Study Limits

The patients’ age, the ethnic and religion considerations, the factors of risk (obesity, diabetes, lipidic disorder, se- dentary lifestyle, stress and alcoholism) as well as the associated pathologies and their number in a same patient have not been taken into consideration in the analysis of the results. The survey was not interested in the undesi- rable events that could occur in the course of the treat- ments and the rate of patients’ adherence to antihyper- tensive drug therapy.

Given that the Ethic Committee was not available at the period of the study, the Ministry of the Health autho- rized the survey.

2.5. Statistical Analyses

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Kruskal-Wallis on Ranks and Dunn’s method (multiple comparison procedures) for DBP control (hospitalized patients).

The control of the BP by pharmacological class com- bination of antihypertensive drugs was compared using: one way ANOVA for SBP and one way ANOVA/ Kruskal-Wallis on Ranks for DBP (ambulatory patients); one way ANOVA for SBP and one way ANOVA/ Bonferroni t-test for DBP (hospitalized patients).

Student t-test and Mann-Whitney Rank Sum Test were used to assess the effect of combination therapy inclu- ding at least one diuretic on mean reduction of SBP/DBP among ambulatory and hospitalized patients.

The difference between the treated groups was consi- dered to be significant if p < 0.05.

3. Results

3.1. Epidemiological Aspect

Of the 204 patients included in the study, 176 were placed on antihypertensive drug therapy; among them 99 were male (56.25%) while 77 females (43.75%) with a sex ratio of 1.3. The average age was 55.01  12.55 years (29 to 87 years). The pattern of treatment was ambula- tory for 82 patients (46.59%) and hospitalized for 94 patients (53.41%); 23 case notes were not used due to incompleteness. Five patients were placed on only die- tary sodium restriction or anxiolytic drugs.

3.2. Blood Pressure Control among Ambulatory Patients

3.2.1. Sex and Ambulatory Status and Blood Pressure Control

The mean and median values of both SBP/DBP reduc- tions under antihypertensive treatment were 44.21/10.00 mmHg for the male and 33.99/15.00 mmHg for the fe- male.

Of the 112 patients who controlled their BP under hy- pertensive treatment, 43 (38.39%) received an ambula- tory treatment. The mean median value of both SBP/DBP reductions due to that treatment was 30.00/15.00 mmHg (Table 1).

3.2.2. Antihypertensive Therapy on Blood Pressure Control among Ambulatory Patients

Thirty five outpatients (81.40%) were placed on combi- nation therapy of whom 23 were on bitherapy (53.49%) and 12 on tritherapy (27.91%). Eight (18.60%) were on monotherapy (Table 2).

These tree antihypertensive regimens were not dif- ferent regarding the mean and median values of both SBP/DBP reductions (Table 3).

[image:3.595.308.538.142.221.2]

The monotherapy made of calcium channel antago-

Table 1. Distribution of patients whose BP was controlled according to the ambulatory or hospitalized status and as- sessment of the effect of this status on the mean SBP/DBP reductions.

SBP reduction (mmHg)

DBP reduction (mmHg)

Treated groups n

Median

value p

Median

value p

Ambulatory

patients 43 30.00 15.00

Hospitalized

patients 69 60.00

0.001

30.00 0.004

[image:3.595.308.539.291.410.2]

SBP: systolic blood pressure; DBP: diastolic blood pressure; n: number of ambulatory and hospitalized patients with controlled BP.

Table 2. Distribution of patients whose BP was controlled according to antihypertensive regimens prescribed among ambulatory or hospitalized patients.

Ambulatory Hospitalized Antihypertensive regimens

n % n %

Bitherapy 23 53.49 27 39.13

Tritherapy 12 27.91 23 33.33

Monotherapy 8 18.60 5 7.25

Quadritherapy - - 13 18.84

 4 antihypertensive drugs

combination - - 1 1.45

Total 43 100.00 69 100.00

n: number of ambulatory and hospitalized patients with controlled BP.

Table 3. Comparison of the effect of antihypertensive regi- mens prescribed on the mean reduction of SBP/DBP among ambulatory patients.

SBP reduction (mmHg)

DBP reduction (mmHg) Antihypertensive

regimens Mean

value p

Median

value p

Bitherapy (n = 23) 34.13 10.00

Tritherapy (n = 12) 38.33 17.50

Monotherapy (n= 8) 48.75

0.295

20.00

0.576

n: number of ambulatory patients with controlled BP.

nists (CCA) and the antihypertensive class combinations such as diuretic (D) + CCA, D + angiotensin converting enzyme inhibitor (ACEI), D + CCA + ACEI were com- parable in term of the mean reduction of both SBP (p = 0.079) and DBP (p = 0.137) (Table 4).

Patients placed on combination therapy including at least one diuretic were 34/35 (97.14%). The median value of SBP/DBP lowering was 30.00/10.00 mmHg (p  0.001) (Table 8).

[image:3.595.308.538.471.558.2]
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Table 4. Comparison of the effect of antihypertensive class combinations on the mean reduction of SBP/DBP among ambulatory patients.

SBP reduction (mmHg)

DBP reduction (mmHg) Antihypertensive class

combinations Mean

value p

Median

value p

CCA (n = 4) 61.250 20.000

D + CCA (n = 4) 45.000 20.000

D + ACEI (n = 13) 29.615 10.000

D +CCA + ACEI (n = 3) 21.665 10.000

Others (n = 19) 40.000

0.079

20.000 0.137

n: number of ambulatory patients with controlled BP.

serpine/spironolactone + altizide.

3.3. Blood Pressure Control among Hospitalized Patients

3.3.1. Sex and Hospitalized Status and Blood Pressure Control

The median and mean values of both SBP/DBP reduc- tions under antihypertensive treatment were 60.00/33.16 mmHg for the male and 60.00/30.97 mmHg for the fe- male.

Of the 112 patients who controlled their BP, 69 (61.61%) were hospitalized. Among them the antihyper- tensive treatment induced both SBP/DBP reductions ex- pressed as the mean median value of 60.00/30.00 mmHg (Table 1).

3.3.2. Antihypertensive Therapy on Blood Pressure Control among Hospitalized Patients

Of the 69 inpatients, 27 were placed on bitherapy (39.13%), 23 on tritherapy (33.33%), 14 on quadritherapy (n = 13) and 4 antihypertensive drugs combination (20.29%) and 5 benefited from monotherapy (Table 2). The combination therapy was applied to 64 patients (92.75%).

The difference in SBP mean reduction was 43.23 mmHg between quadritherapy and monotherapy (p = 0.043), 35.89 mmHg between quadritherapy and bitherapy (p = 0.004) and 26.18 mmHg between quadritherapy and tri- therapy (p = 0.079) (Table 5). The difference of ranks of DBP mean reduction between the four regimens were in

Table 5. The median values of DBP mean reduction

were: 10 mmHg (monotherapy), 20 mmHg (bitherapy), 30 mmHg (tritherapy) and 40 mmHg (quadrictherapy) (p = 0.023).

The combinations including D + CCA, D + ACEI, D + CCA + ACEI and D + CCA + ACEI + CAAD induced mean values of SBP reduction represented in Table 6 (p = 0.121). The quadruple combination exerted a DBP mean reduction of 38.39 mmHg (difference of ranks) compared to D + CCA-based combination (p = 0.015). All other combinations were comparable concerning the

Table 5. Comparison of the effect of antihypertensive regi- mens prescribed on the mean reduction of SBP/DBP among hospitalized patients.

SBP reduction (mmHg)

DBP reduction (mmHg) Antihypertensive

regimens prescribed Difference

of means p

Difference

of ranks p

Quadritherapy (n = 13)

vs Monotherapy (n = 5) 43.231 0.043 26.462 NS

Quadritherapy (n = 13)

vs Bitherapy (n = 27) 35.897 0.004 17.165 NS

Quadritherapy (n = 13)

vs Tritherapy (n = 23) 26.187 0.079 10.940 NS

Tritherapy (n = 23)

vs Monotherapy (n = 5) 17.043 1.000 15.522 NS

Tritherapy (n = 23)

vs Monotherapy (n = 5) 9.710 1.000 6.225 NS

Monotherapy (n = 5)

vs Bitherapy (n = 27) 7.333 1.000 9.296 NS

vs: versus; n: number of hospitalized patients with controlled BP; NS: no significant.

Table 6. Comparison of the effect of antihypertensive class combinations on the mean reduction of SBP among hospi- talized patients.

SBP reduction (mmHg) Antihypertensive class

combination

Mean value  SEM p

D + CCA (n = 7) 52.143  5.759

D + ACEI (n = 11) 55.000  7.949

D + ACEI + CCA (n = 9) 61.111  30.596

D + ACEI + CCA + CAAD (n = 8) 90.000  26.186

Others (n = 33) 61.818  35.747

0.121

D: diuretic; CCA: calcium channel antagonist; ACEI: angiotensin-convert- ing enzyme inhibitor; CAAD: centrally acting antihypertensive drug; n = number of hospitalized patients with controlled BP; SEM: standard error of mean.

difference of ranks (Table 7).

Patients placed on combination therapy including at least one diuretic were 56 out of 64 (87.50%). The me-dian value of SBP/DBP lowering was 60.00/30.00 mmHg (Table 8).

The molecules and fixe combinations which were pre- ferentially prescribed in decreasing frequency were: fu- rosemide, nicardipine, captopril,  methyldopa, hydro- chlorothiazide + captopril, atenolol/indapamide and clo- nidine.

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[image:5.595.59.288.133.395.2]

Table 7. Comparison of the effect of antihypertensive class combinations on the mean reduction of DBP among hospi- talized patients.

DBP reduction (mmHg) Antihypertensive class

combination prescribed Difference of

ranks p

D + CCA + ACEI + CAAD (n = 8)

vs D + CCA (n = 7) 38.393 0.015

D + CCA + ACEI + CAAD (n = 8)

vs others (n = 33) 19.129 0.334

D + CCA + ACEI + CAAD (n = 8)

vs D + ACEI (n = 11) 18.523 0.789

D + CCA + ACEI + CAAD (n = 8)

vs D + CCA + ACEI (n = 9) 15.694 1.000

D + CCA + ACEI (n = 9)

vs D + CCA (n = 7) 22.698 0.478

D + CCA + ACEI (n = 9)

vs others (n = 33) 3.434 1.000

D + CCA + ACEI (n = 9)

vs D + ACEI (n = 11) 2.828 1.000

D + ACEI (n = 11)

vs D + CCA (n = 7) 19.870 0.702

D + ACEI (n = 11)

vs others (n = 33) 0.606 1.000

Others (n = 33)

vs D + CCA (n = 7) 19.262 0.421

D: diuretic; CCA: Calcium channel antagonist; ACEI: angiotensin-convert- ing enzyme inhibitor; CAAD: centrally acting antihypertensive drug; n: number of hospitalized patients with controlled BP.

Table 8. Comparison of the effect of antihypertensive class combinations including at least one diuretic on SBP/DBP control among ambulatory and hospitalized patients.

SBP reduction (mmHg)

DBP reduction (mmHg) Antihypertensive class

combinations including at

least one diuretic Median

value p

Median

value p

Ambulatory patients

(n = 34) 30.000 10.000

Hospitalized patients

(n = 56) 60.000

0.001

30.000 0.001

n: number of ambulatory and hospitalized patients with controlled BP.

4. Discussion

Our series is essentially urban and does not pretend by that fact to represent the whole Togolese population.

In our study, men (57.39%) seem more affected by HBP than women (43.18%) with male to female ratio of 1.3:1 while Etuk et al. [16] in Nigeria reported a ratio of 1:1.2. However, the average age of 55.01  12.55 years is a bit higher than the one referred to in the study by the previous cited author (52.6  14.6 years) [16].

Our study showed that, globally, out of 176 patients placed on antihypertensive treatment, the disease was controlled among 112 (63.64%) patients or 36.36% of

resistance to the treatment. That failure rate is a bit lower if we consider the definition of the resistant or refractory HBP: a HBP is said to be refractory when a treatment in- cluding hygieno-dietetic measures and the prescription of a drug combination consisting of at least 3 antihyperten- sive drugs one of which, an adequate dose of diuretic did not succeed in lowering the SBP and DBP less than 140/90 mmHg [17-19]. In our series, 25 patients out of 72 (34.72%) have been in that figure case.

These results issued from outpatients and inpatients could not be compared to that from Nigeria which situ- ated the rate of BP control among outpatients at 29.0% and 30.5% [16,20] according to two studies.

Regarding the sex factor impact (hormonal and phy- siopathological differences) on SBP and DBP reduction on antihypertensive treatment, we did not observe any statistically significant difference between mean and me- dian values of both sexes among outpatients (p = 0.142 for SBP and p = 0.922 for DBP) and inpatients (p = 0.647 for SBP and p = 0.711 for DBP). For lack of data in the literature, our results have not been able to be com- pared to other studies.

Among patients whose BP was controlled, 38.39% (n = 43) were placed on ambulatory treatment while 61.61% (n = 69) were hospitalized. The comparison of mean me- dian values of SBP/DBP showed a statistically signifi- cant difference between treated patients (p = 0.001 for SBP and p = 0.004 for DBP). That difference could be explained by the poor adherence to treatment, the non respect of the hygieno-dietetic measures by the patients on ambulatory treatment.

It is generally admitted that the HBP management starts by monotherapy at an efficient dose which is going to be a substitute for combinations which are recom- mended in recent tendencies as first line treatment [20- 22]. The bitherapy was at the top of prescriptions having allowed to control the disease in 53.49% of ambulatory patients against 39.13% of hospitalized patients. Only hospitalized patients were placed on quadritherapy or 4 antihypertensive drugs combination with 20.29% of BP control. Indeed, the patients were often admitted urgently in the hospital with a severe or complicated HBP or when through a failure stage of monotherapy, bitherapy or tritherapy, hence the necessity to use more than 3 mo- lecules to control BP. That result confirms the one re- ferred to by Etuk et al. [16] who preconized the mono- therapy, the tritherapy or the quadritherapy from moder- ate to severe HBP respectively.

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referred to numerous clinical trials in which the majority of patients needed a treatment with the combination of several antihypertensive agents [8,23-25].

The treated groups placed on hypertensive regimens (monotherapy, bitherapy and tritherapy) among ambula-tory patients were comparable regarding the mean values of SBP reduction (p = 0.295) and the median values of DBP reduction (p = 0.576). Whereas, quadritherapy in-duced a significant lowering of SBP compared to mono-therapy (p = 0.043) and bimono-therapy (p = 0.004) among hospitalized patients. Those results could be explained by a poor adherence of outpatients and a more important resort to quadritherapy in hospitalized patients, whose level of adherence was probably better (61.61% of BP control).

The lack of significant difference of tritherapy com- pared to bitherapy and to monotherapy among the two categories of patients, could also be explained by the poor adherence of patients. As a matter of fact, the com- bination of various molecules negatively influences pa- tients’ adherence and consequently BP control [26]; that could explain this apparent lack of difference between the combinations of two molecules compared to mono- therapy and of 3 molecules compared to bitherapy [16] or to monotherapy.

The combinations including D + ACEI, D + CCA, D + ACEI + CCA and monotherapy made of CCA were comparable regarding their effect on SBP/DBP control among ambulatory patients. Those combinations includ- ing the quadruple therapy and excluding CCA induced no significant SBP mean reduction while the quadrithe- rapy comprising D + CCA + ACEI + CAAD exerted a significant DBP mean reduction (p = 0.015) among hos- pitalized patients compared to D + CCA-based combina- tion. That finding confirms partially the fact that D + CCA seem the combination the least synergic on both the SBP and DBP because of its partially additive BP reduc- tion [27,28]. That result corroborates those of other au- thors [29,30] who criticize the synergic effect of that combination. Furthermore, it does not count among the “preferred”[15] combinations including ACEI/antagonist of receptor of angiotensin II (ARA II) + D or ACEI/ARA II + CCA combination [15,23,31]; however, that combi- nation is classified as “acceptable” [15]. Among the two categories of hypertensive patients, D + ACEI-based combination was not superior to D + CCA as a partially additive BP reduction combination [32-34]and CCA as monotherapy, despite the fact that, that combination re- sults in fully additive BP reduction [35-39].

In the present study, the bitherapies including D + ACEI and D + CCA-based combinations were the most frequently prescribed; So the patterns of prescription were in accordance with the European revised directives

[40] which recommend a diuretic and a CCA or a renin angiotensin system antagonist (ACEI or ARA II) or a CCA and a renin angiotensin system antagonist whereas the Joint National Committee (JNC)—7 of 2003 (USA) usually recommends a diuretic in the strategy associating two antihypertensive drugs [8].

The tritherapy which came to the second position of prescriptions (two folds in hospitalized conditions) was not statistically more efficient than monotherapy or bi- therapy on the BP reduction. According to JNC-7, in case of bitherapy inefficiency, the optimization of doses or combination to a supplementary antihypertensive drug is recommended [17]. The European directives of 2009 de- creed the following: When a tritherapy is necessary, the most rational combination seems to be an angiotensin sy- stem antagonist, a CCA and a diuretic at efficient doses [40]. As a matter of fact, the BP reduction obtained with vessel-dilating agents (CCA and ACEI) always induces secondary salts and water retention; hence the interest to associate the diuretics, even their effectiveness on SBP and DBP reduction is less compared to ACEI [41] or CCA [16,41]. Our results agree with European directive: the D + CCA + ACEI combination including 3 major classes of antihypertensive drugs used at the first inten- tion [42] obtained the prescribers preference (12/35). That combination is particularly beneficial to black hy- pertensive patients; indeed, it has been shown that, that combination improved the BP control as well as the car- dio and reno protection [2,43-46]. However, in England and in other European countries, the renin angiotensin system blockers are not recommended at initial treatment in the black race patients [47].

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notherapy.

All the combinations of quadritherapy used consisted of a diuretic. According to Achard et al. [29], the resort to quadritherapy supposes that the prescriber kept away all the etiology including those of secondary HBP. In that case, the therapeutic procedure will be guided by the analysis of the pressure mechanisms responsible for the resistance to treatment: systolic output, peripheral resis- tance, sodium concentration, catecholamines activity, renin and aldosterone activity. The same author appends that in principle, despite that analysis, empiricism sometimes re- mains the single recourse. That empiricism coupled with the difficulty in the management of HBP has been em- phasized by other authors: The HBP control remains pro- blematic despite the existence of algorithms allowing to predict the patients’ individual response to different groups of antihypertensive drugs [50]; the variability in patients’ individual responses to different groups of antihyperten- sive drugs [50]; the therapeutic inertia [8]; the compen- satory responses to antihypertensive treatment [15]; the non respect sometimes in the implementation of JNC 7’s recommendations [13,51]. Furthermore, the high and more and more increasing number of hypertensive pati- ents despite the enormous progress in term of HBP treat- ment, remains a paradox [52].

In conclusion, the results of our study agree with the data of the literature; as the matter of fact, the diuretics, the calcium channel antagonists and the angiotensin con- verting enzyme inhibitors constitute the 3 groups of the first line antihypertensive drugs in the treatment of es- sential HBP in our context (patient of black race, ambu- latory and hospitalized conditions). The tree pharmaco- logical groups were used in monotherapy, but often in combination with 1, 2, 3 even 4 antihypertensive drugs belonging to other pharmacological groups. However, the D + CCA combination which came to the second position of prescriptions of bitherapy seemed the least synergic. That finding must be taken into account by pre- scribers. The strategy combining 4 antihypertensive drugs (D + CCA + ACEI + CAAD) used for inpatients reduced significantly the mean DBP compared to D + CCA-based combination. The present study allowed thus to make available important pre-requisites for further additional investigations in order to identify the combinations that is most likely to be beneficial to majority of hypertensive patients.

REFERENCES

[1] A. A. Lopes, “Hypertension in Black People: Patho- physiology and Therapeutic Aspects. Journal of Human

Hypertension, Vol. 16, No. 1, 2002, pp. 11-12.

doi:10.1038/sj.jhh.1001333

[2] J. G. Douglas and L. Agodoa, “ACE Inhibition Is Ef- fective and Renoprotective in Hypertensive Nephro- sclerosis: The African American Study of Kidney Disease and Hypertension (AASK) Trial,” Kidney International

Supplements,Vol. 63, Suppl. 83, 2003, pp. 74-76.

[3] B. L. Salako, F. A. Ajose and E. Lawani, “Blood Pressure Control in a Population Where Antihypertensives Are Given Free,” East African Medical Journal, Vol. 80, No. 10, 2003, pp. 529-531.

[4] S. A. Isezuo and C. H. Njoku, “Blood Pressure Control among Antihypertensives Managed in a Specialized Health Care Sitting in Nigeria,” African Journal of Medicine &

Medical Sciences, Vol. 32, 2003, pp. 65-70.

[5] S. A. Isezuo and T. C. Opera, “Hypertension Awareness among Nigerian Hypertensives in a Nigerian Tertiary Health Institution,” Sahel Medical Journal, Vol. 3, No. 2, 2000, pp. 93-97.

[6] D. J. Hyman and V. N. Pavlik, “Characteristics of Patients with Uncontrolled Hypertension in the United States,” The New England Journal of Medicine, Vol. 345, No. 7, 2001, pp. 479-486. doi:10.1056/NEJMoa010273 [7] X. S. Ren, L. E. Kazis, A. Lee, H. Zhang and D. R. Miller,

“Identifying Patient and Physician Characteristics That Effect Compliance with Antihypertensive Medications,”

Journal of Clinical Pharmacy and Therapeutics, Vol. 27,

No. 1, 2002, pp. 47-56.

doi:10.1046/j.1365-2710.2002.00387.x

[8] R. Düsing, “Optimizing Blood Pressure Control through the Use of Fixed Combinations,” Vascular Health and

Risk Management, Vol. 6, 2010, pp. 321-325.

[9] F. Damorou, E. Togbossi, F. Pessinaba and B. Soussou, Epidemiology and Diagnostic Circumstances of Arterial Hypertension in the Hospital Environment in Kpalime (Second Largest City in Togo),” Mali Medical, Vol. 23, No. 4, 2008, pp. 17-20.

[10] F. Damorou, F. Pessinaba, T. Tcherou, K. Yayehd, S. M. Ndassa and B. Soussou, “Arterial Hypertension in Black Subjects over 50 Years of Age in Lomé: Epidemiological Aspects and Evaluation of Cardiovascular Risk (Pros- pective and Longitudinal Study of 1485 Patients),” An-

nales de Cardiologie et dAngéiologie (Paris), Vol. 60,

No. 2, 2011, pp. 61-66.

[11] C. P. Page, M. J. Curtis, M. J. Walker, M. C. Sutter and B. B. Hoffman, “Integrated Pharmacology,” 1st Edition, De- Boeck Université, Paris, 1999.

[12] E. Poluzzi, P. Strahinja, A. Vargiu, G. Chiabrando, M. C. Silvani, D. Motola, G. S. Cellini, A. Vaccheri, F. de Ponti and N. Montanaro, “Initial Treatment of Hypertension and Adherence to Therapy in General Practice in Italy,”

European Journal of Clinical Pharmacology, Vol. 61, No.

8, 2005, pp. 603-609. doi:10.1007/s00228-005-0957-y [13] B. A. Staffileno, “Treating Hypertension with Cardiopro-

tective Therapies, the Role of ACE Inhibitors, ARBs, and Beta-Blockers,” Journal of Cardiovascular Nursing, Vol. 20, No. 5, 2005, pp. 354-364.

(8)

zinische Klinik (Munich), Vol. 98, No. 12, 2003, pp. 771- 775. doi:10.1007/s00063-003-1323-4

[15] A. H. Gradman, J. N. Basile, B. L. Carter and G. L. Ba- kris, “Combination Therapy in Hypertension,” The Jour-

nal of Clinical Hypertension, Vol. 13, No. 3, 2011, pp.

146-154. doi:10.1111/j.1751-7176.2010.00397.x

[16] E. Etuk, S. A. Isezuo, A. Chika, J. Akuche and M. Ali, “Prescription Pattern of Anti-Hypertensive Drugs in a Tertiary Health Institution in Nigeria,” Annals of African

Medicine, Vol. 7, No. 3,2008, pp. 128-132.

doi:10.4103/1596-3519.55665

[17] A. V. Chobanian, G. L. Bakris, H. R. Black, W. C. Cush- man, L. A. Green, J. L. Izzo Jr., D. W. Jones, B. J. Mater- son, S. Oparil, J. T. Wright Jr., E. J. Roccella and The National High Blood Pressure Education Program Co- ordinating Committee, “Seventh Report of the Joint Na- tional Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure,” Journal of the

American Medical Association, Vol. 289, No. 19, 2003,

pp. 2560-2572. doi:10.1001/jama.289.19.2560

[18] J. F. Setaro and H. R. Black, “Refractory Hypertension,”

New England Journal of Medicine, Vol. 327, No. 8, 1992,

pp. 543-547. doi:10.1056/NEJM199208203270808 [19] The Task Force for the Management of Arterial Hyper-

tension of the European Society of Hypertension (ESH) ESH and ESC and of the European Society of Cardiology. Guidelines for the Management of Arterial Hypertension.

Journal of Hypertension, Vol. 25, No. 6, 2007, pp. 1105-

1187. doi:10.1097/HJH.0b013e3281fc975a

[20] K. B. Yusuff and O. Balogun, “Physicians Prescribing of Antihypertensive Combinations in Tertiary Care Setting in Southwestern Nigeria,” Journal of Pharmaceutical Sci-

ences, Vol. 8, No. 2, 2005, pp. 235-242.

[21] I. Gavras and T. Tsenthal, “Combination Therapy as First- Line Treatment for Hypertension,” Current Hypertension

Reports, Vol. 6, No. 4, 2004, pp. 267-272.

doi:10.1007/s11906-004-0020-x

[22] J. M. Neutel, “The Role of Combination Therapy in the Management of Hypertension,” Nephrology Dialysis Trans-

plantation, Vol. 21, No. 6, 2006, pp. 1469-1473.

doi:10.1093/ndt/gfk064

[23] A. V. Chobanian, G. L. Bakris, H. R. Black, W. C. Cush- man, L. A. Green, J. L. Izzo Jr., D. W. Jones, B. J. Mater- son, S. Oparil, J. T. Wright Jr. and E. J. Roccella, “Se- venth Report of the Joint National Committee on Pre- vention, Detection, Evaluation and Treatment of High Blood Pressure,” Hypertension, Vol. 42, No. 6, 2003, pp. 1206-1252. doi:10.1161/01.HYP.0000107251.49515.c2 [24] L. Hanson, A. Zanchetti, S. G. Carruthers, B. Dahlöf, D.

Elmfeldt, S. Julius, J. Ménard, K. H. Rahn, H. Wedel and S. Westerling, “Effects of Intensive Blood Pressure Lower- ing and Low-Dose Aspirin in Patients with Hypertension: Principal Results of the Hypertension Optimal Treatment (HOT) Randomized Trial,” Lancet, Vol. 351, No. 9118, 1998, pp. 1755-1762.

doi:10.1016/S0140-6736(98)04311-6

[25] J. Chalmer, “The ABCD of Antihypertensive Therapy?”

Journal of Hypertension, Vol. 20, No. 4, 2002, pp. 615-

616. doi:10.1097/00004872-200204000-00016

[26] J. G. Douglas, G. L. Bakris, M. Epstein, K. C. Ferdinand, C. Ferrario, J. M. Flack, K. A. Jamerson, W. E. Jones, J. Haywood, R. Maxey, E. O. Ofili, E. Saunders, E. L. Schi- ffrin, D. A. Sica, J. R. Sowers and D. G. Vidt, “Manage- ment of High Blood Pressure in African Americans: Con- sensus Statement of the Hypertension in African Ame- ricans. Working Group of the International Society on Hypertension on Blacks,” Archives of Internal Medicine, Vol. 163, No. 5, 2003, pp. 525-541.

doi:10.1001/archinte.163.5.525

[27] A. Salvetti, A. Magagna, P. Innocenti, F. Ponzanelli, A. Cagianelli, M. Cipriani, E. Gandolfi, C. Del Prato, A. M. Ballestra, P. Saba, F. Giuntoli, G. Panebianco and S. Amigoni, “The Combination of Chlorthalidone with Nife- dipine Does Not Exert an Additive Antihypertensive Ef- fect in Essential Hypertensives: A Crossover Multicenter Study,” Journal of Cardiovascular Pharmacology, Vol. 17, No. 2, 1991, pp. 332-335.

doi:10.1097/00005344-199102000-00021

[28] M. R. Weir, M. A. Weber, H. A. Punzi, H. M. Serfer, S. Rosenblatt and W. J. Cady, “A Dose Escalation Trial Comparing the Combination of Diltiazem SR and Hydro- chlorothiazide with the Monotherapies in Patients with Essential Hypertension,” Journal of Human Hypertension, Vol. 6, No. 2, 1992, pp. 133-138.

[29] J. M. Achard and A. Fournier, “Facteurs de Résistance au Traitement d’une HTA,” Revue du Praticien, Vol. 14, 1993, pp. 1813-1819.

[30] C. Thuillez, “Inhibiteurs Calciques,” Revue du Praticien, Vol. 9, 1993, pp. 1163-1165.

[31] A. H. Gradman, J. N. Basile, B. L. Carter, G. L. Brakis, B. J. Materson, H. R. Black, J. L. Izzo Jr., S. Oparil and M. A. Weber, “Combination Therapy in Hypertension,” Jour-

nal of the American Society of Hypertension, Vol. 4, No.

2, 2010, pp. 90-98. doi:10.1016/j.jash.2010.03.001 [32] W. H. Frishman, C. V. S. Ram, F. G. McMahon, S. G.

Chrysant, A. Graff, J. W. Kupiec and H. Hsu, “Com- parison of Amlodipine and Benazepril Monotherapy to Amlodipine plus Benazepril in Patients with Systemic Hypertension: A Randomized, Double-Blind, Placebo- Controlled, Parallel-Group Study,” The Journal of Cli-

nical Pharmacology, Vol. 35, No. 11, 1995, pp. 1060-

1066.

[33] T. Philipp, T. R. Smith, R. Glazer, M. Wernsing, J. Yen, J. Jin, H. Schneider and R. Pospiech, “Two Multicenter, 8- Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Studies Evaluating the Efficacy and To- lerability of Amlodipine and Valsartan in Combination and as Monotherapy in Adult Patients with Mild to Mo- derate Essential Hypertension,” Clinical Therapeutics, Vol. 29, No. 4, 2007, pp. 563-580.

doi:10.1016/j.clinthera.2007.03.018

(9)

rapeutics, Vol. 30, No. 4, 2008, pp. 587-604. doi:10.1016/j.clinthera.2008.04.002

[35] S. G. Chrysant, “Antihypertensive Effectiveness of Low- Dose Lisinopril Hydrochlorothiazide Combination,” Ar-

chives of Internal Medicine, Vol. 154, No. 7, 1994, pp.

737-743. doi:10.1001/archinte.154.7.737

[36] S. G. Chrysant, T. Fagan, R. Glazer and A. Kriegman, “Effects of Benazepril and Hydrochlorothiazide, Given Alone and in Low- and High-Dose Combinations, on Blood Pressure in Patients with Hypertension,” The An-

nals of Family Medicine, Vol. 5, No. 1, 1996, pp. 17-24.

doi:10.1001/archfami.5.1.17

[37] J. Pool, W. C. Cushman, R. K. Saini, C. E. Nwachuku and J. P. Battikha, “Use of the Factorial Design and Qua- dratic Response Surface Models to Evaluate the Fosi- nopril and Hydrochlorothiazide Combination Therapy in Hypertension,” American Journal of Hypertension, Vol. 10, No. 1, 1997, pp. 117-123.

doi:10.1016/S0895-7061(96)00323-8

[38] A. H. Gradman and R. Kad, “Renin Inhibition in Hyper- tension,” Journal of the American College of Cardiology, Vol. 51, No. 5, 2008, pp. 519-528.

doi:10.1016/j.jacc.2007.10.027

[39] J. H. Mackay, K. E. Arcuri, A. I. Goldberg, S. M. Sna- pinn and C. S. Sweet, “Losartan and Low-Dose Hydro- chlorothiazide in Patients with Essential Hypertension,”

Archives of Internal Medicine, Vol. 156, No. 3, 1996, pp.

278-285. doi:10.1001/archinte.1996.00440030072009 [40] G. Mancia, S. Laurent, E. Agabiti-Rosei, E. Ambrosioni,

M. Burnier, M. J. Caulfield, R. Cifkova, D. Clément, A. Coca, A. Dominiczak, S. Erdine, R. Fagard, C. Farsang, G. Grassi, H. Haller, A. Heagerty, S. E. Kjeldsen, W. Kiowski, J. M. Mallion, A. Manolis, K. Narkiewicz, P. Nilsson, M. H. Olsen, K. H. Rahn, J. Redon, J. Rodicio, L. Ruilope, R. E. Schmieder, H. A. Struijker-Boudier, P. A. van Zwieten, M. Viigimaa and A. Zanchetti, “Reappraisal of European Guidelines on Hypertension Management: An European Society of Hypertension Task Force Do- cument,”Journal of Hypertension, Vol. 27, No. 11, 2009, pp. 2121-2158. doi:10.1097/HJH.0b013e328333146d [41] M. Veronesi, A. F. G. Cicero, M. G. Prandin, A. Dormi,

E. Cosentino, E. Strocchi and C. Borghi, “A Prospective Evaluation of Persistence on Antihypertensive Treatment with Different Antihypertensive Drugs in Clinical Pra- ctice,” Vascular Health and Risk Management, Vol. 3, No. 6, 2007, pp. 1000-1005.

[42] J. T. Wright Jr., J. K. Dunn, J. A. Cutler, B. R. Davis, W. C. Cushman, C. E. Ford, L. J. Haywood, F. H. Leenen, K. L. Margolis, V. Papademetriou, J. L. Probstfield, P. K. Whelton and G. B. Habib, “Outcomes in Hypertensive Black and Nonblack Patients Treated with Chlorthalidone, Amlodipine, and Lisinopril,” Journal of the American

Medical Association, Vol. 293, No. 13, 2005, pp. 1595-

1608. doi:10.1001/jama.293.13.1595

[43] D. E. Bild, D. A. Bluemke, G. L. Burke, R. Detrano, A. V. D. Roux, A. R. Folsom, P. Greenland, D. R. Jacob Jr., R. Kronmal, K. Liu, J. C. Nelson, D. O’Leary, M. F. Saad, S. Shea, M. Szklo, R. P. Tracy, “Multi-Ethnic Study of Atherosclerosis, Objective and Design,” American Jour-

nal of Epidemiology, Vol. 156, No. 9,2002, pp. 871-881.

doi:10.1093/aje/kwf113

[44] A. Fenves and C. V. Ram, “Are Angiotensins Converting Enzyme Inhibitors and Angiotensin Receptor Blokers Be- coming the Treatment of Choice in African-American?”

Current Hypertension Reports, Vol. 4, No. 4, 2002, pp.

286-289. doi:10.1007/s11906-996-0006-y

[45] M. Rahman, “Initial Findings of the AASK, African Ame- ricans Kidney Benefit from an ACE Inhibitor,” Cleveland

Clinic Journal of Medicine, Vol. 70, No. 4, 2003, pp.

304-305. doi:10.3949/ccjm.70.4.304

[46] L. Hanson, L. H. Lindholm, L. Niskanen, J. Lanke, T. Hed- ner, A. Niklason, K. Luomanmäki, B. Dahlöf, U. de Faire, C. Mörlin, B. E. Karlberg, P. O. Wester and J. E. Björck, “Effect of Angiotensin Converting Enzyme Inhibition Com- pared with Conventional Morbidity and Mortality in Hy- pertension: The Captopril Prevention Project (CAPPP) Randomized Trial,” Lancet, Vol. 353, No. 9153,1999, pp. 611-616. doi:10.1016/S0140-6736(98)05012-0

[47] J. L. Izzo Jr. and A. S. Zion, “Combined Aliskiren-Amlo- dipine Treatment for Hypertension in African Americans Clinical Science and Management Issues,” Therapeutic

Advances in Cardiovascular Disease, Vol. 5, No. 3, 2011,

pp. 169-1725. doi:10.1177/1753944711409615

[48] E. Saunders, “Hypertension in Blacks,” Primary Care, Vol. 18, 1881, pp. 607-622.

[49] L. A. Salako, “Hypertension in Africa and Effectiveness of Its Management with Various Classes of Antihyper- tensive Drugs and in Different Socio-Economic and Cul- tural Environments,” Clinical and Experimental Hyper-

tension, Vol. 15, No. 6,1993, pp. 997-1004.

doi:10.3109/10641969309037087

[50] L. Welsh and A. Ferro, “Drug Treatment of Essential Hy- pertension: The Case for Initial Combination Therapy,”

International Journal of Clinical Practice, Vol. 58, No.

10, 2004, pp. 956-963.

doi:10.1111/j.1368-5031.2004.00392.x

[51] S. A. Revaz, A. Morabia, C. Goehring and H. Stalder, “Eva- luation of Drug Prescription in the Primary Care Clinic in Geneva in 1997,” Schweiz Med Wochenschr, Vol. 129, No. 49, 1999, pp. 1935-1937.

[52] A. V. Chobanian, “The Hypertension Paradox—More Un- controlled Disease despite Improved Therapy,” The New

England Journal of Medicine, Vol. 361, No. 9,2009, pp.

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Abreviations

HBP: High blood pressure; BP: Blood pressure;

SBP: Systolic blood pressure; DBP: Diastolic blood pressure; D: Diuretic;

CCA: Calcium channel antagonist;

ACEI: Angiotensin-converting enzyme inhibitor; CAAD: Centrally acting antihypertensive drug; ARA II: Antagonist of receptor of angiotensin II; n = Number of patients treated;

Figure

Table 2. Distribution of patients whose BP was controlled according to antihypertensive regimens prescribed among ambulatory or hospitalized patients
Table 7. Comparison of the effect of antihypertensive class combinations on the mean reduction of DBP among hospi- talized patients

References

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